首页> 外国专利> METHOD AND KIT FOR DETECTING RNA N6-METHYLADENINE MODIFICATION AT SINGLE-BASE RESOLUTION IN RANGE OF WHOLE TRANSCRIPTOME

METHOD AND KIT FOR DETECTING RNA N6-METHYLADENINE MODIFICATION AT SINGLE-BASE RESOLUTION IN RANGE OF WHOLE TRANSCRIPTOME

机译:在整个转录组范围内的单碱分辨率下检测RNA N6-甲基腺嘌呤改性的方法和试剂盒

摘要

Disclosed is a method and kit for detecting an RNA N6-methyladenine modification at a single-base resolution in the range of a whole transcriptome. According to the method, on the basis of an N6-allyl label of in-vivo ribonucleic acid (RNA) adenine and a chemical treatment, base mutation of the in-vivo RNA adenine in the process of reverse transcription into DNA is induced, and a mutation site is then recognized by means of nucleic acid sequencing, so that an a6A site is obtained, wherein the site is a site originally modified by m6A in cell RNA. By means of the method, the specific label of N6-allyladenine in a cell is achieved for the first time, and the label can not only be used for replacing an N6-methyladine site in the cell, but also can be positioned by means of mutation sequencing.
机译:公开了一种用于在整个转录组的范围内以单碱分辨率检测RNA n 6 -methyladenine修饰的方法和试剂盒。根据该方法,基于体内核糖核酸(RNA)腺苷酸(RNA)腺苷酸和化学处理的N 6 -allyl标记,在此过程中,体内RNA腺嘌呤的基础突变诱导逆转录到DNA中,然后通过核酸测序识别突变位点,从而获得A 6 的位点,其中所述位点是最初由m 细胞RNA中的6 a。借助于该方法,首次实现细胞中N 6 -allyladenine的特定标记,并且标签不仅可以用于更换n 6 - 细胞中的甲氨酸位点,但也可以通过突变测序定位。

著录项

  • 公开/公告号WO2021042883A1

    专利类型

  • 公开/公告日2021-03-11

    原文格式PDF

  • 申请/专利权人 ZHEJIANG UNIVERSITY;

    申请/专利号WO2020CN102643

  • 发明设计人 LIU JIANZHAO;FENG XINHUA;SHU XIAO;CAO JIE;

    申请日2020-07-17

  • 分类号C12Q1/6809;C12Q1/6869;G01N33/53;

  • 国家 CN

  • 入库时间 2022-08-24 17:41:44

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